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It is recommended that you apply well in advance as the service is subject to the availability of resources at any given time.
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Approval of the Research Ethics Committee (CEIm) is required
We inform you that any study, whether prospective or retrospective, that uses information relating to the health of individuals (clinical data, complementary examinations, analytical, radiological or imaging data, treatments, etc.) requires the approval of the Research Ethics Committee.
This is established by Royal Decree 1090/2015 for clinical trials, Royal Decree 957/2020 for observational studies with medicines and/or medical devices, and the Biomedical Research Act for all other research projects on human beings or biological material.
Remember that the request for approval from the Ethics Committee must be submitted at the start of the research, as the Committee does not make decisions on research that has already been carried out.
We inform you that any study, whether prospective or retrospective, that uses information relating to the health of individuals (clinical data, complementary examinations, analytical, radiological or imaging data, treatments, etc.) requires the approval of the Research Ethics Committee.
This is established by Royal Decree 1090/2015 for clinical trials, Royal Decree 957/2020 for observational studies with medicines and/or medical devices, and the Biomedical Research Act for all other research projects on human beings or biological material.
Remember that the request for approval from the Ethics Committee must be submitted at the start of the research, as the Committee does not make decisions on research that has already been carried out.